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ethylnitrosourea and Metabolism, Inborn Errors

ethylnitrosourea has been researched along with Metabolism, Inborn Errors in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adamczewska-Goncerzewicz, Z; Mularek, O; Wender, M; Zórawski, A	1
Barnett, LB; Erickson, RP; Lewis, SE; Tashian, RE; Venta, PJ	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Metabolism, Inborn Errors

Article	Year
The fatty acid pattern of central myelin lipids after transplacental intoxication by ethylnitrosourea. Experimental pathology, 1981, Volume: 19, Issue:4 Topics: Abnormalities, Drug-Induced; Animals; Brain; Central Nervous System; Ethylnitrosourea; Fatty Acids; Female; Lipid Metabolism; Maternal-Fetal Exchange; Metabolism, Inborn Errors; Mice; Myelin Sheath; Nitrosourea Compounds; Pregnancy	1981
N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome. Proceedings of the National Academy of Sciences of the United States of America, 1988, Volume: 85, Issue:6 Topics: Alleles; Animals; Carbonic Anhydrases; Chromosomes, Human, Pair 3; Disease Models, Animal; Ethylnitrosourea; Female; Genes; Humans; Immunodiffusion; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mutation; Osteopetrosis	1988

Article

Year

The fatty acid pattern of central myelin lipids after transplacental intoxication by ethylnitrosourea.

Experimental pathology, 1981, Volume: 19, Issue:4

Topics: Abnormalities, Drug-Induced; Animals; Brain; Central Nervous System; Ethylnitrosourea; Fatty Acids; Female; Lipid Metabolism; Maternal-Fetal Exchange; Metabolism, Inborn Errors; Mice; Myelin Sheath; Nitrosourea Compounds; Pregnancy

1981

N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.

Proceedings of the National Academy of Sciences of the United States of America, 1988, Volume: 85, Issue:6

Topics: Alleles; Animals; Carbonic Anhydrases; Chromosomes, Human, Pair 3; Disease Models, Animal; Ethylnitrosourea; Female; Genes; Humans; Immunodiffusion; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mutation; Osteopetrosis

1988